WO1996010439A1 - Interface pour administration iontophoretique transcutanee, et agent et methode de traitement de la peau a cette fin - Google Patents

Interface pour administration iontophoretique transcutanee, et agent et methode de traitement de la peau a cette fin Download PDF

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Publication number
WO1996010439A1
WO1996010439A1 PCT/JP1995/002000 JP9502000W WO9610439A1 WO 1996010439 A1 WO1996010439 A1 WO 1996010439A1 JP 9502000 W JP9502000 W JP 9502000W WO 9610439 A1 WO9610439 A1 WO 9610439A1
Authority
WO
WIPO (PCT)
Prior art keywords
drug
skin
interface
iontophoresis
solution
Prior art date
Application number
PCT/JP1995/002000
Other languages
English (en)
French (fr)
Japanese (ja)
Inventor
Keiichiro Okabe
Shinichi Sunahori
Emi Kyo
Original Assignee
Kabushiki Kaisya Advance
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP25967794A external-priority patent/JP2818771B2/ja
Priority claimed from JP33280694A external-priority patent/JP2909483B2/ja
Application filed by Kabushiki Kaisya Advance filed Critical Kabushiki Kaisya Advance
Priority to US08/649,583 priority Critical patent/US5894021A/en
Priority to EP95932949A priority patent/EP0739644A4/de
Publication of WO1996010439A1 publication Critical patent/WO1996010439A1/ja

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N1/00—Electrotherapy; Circuits therefor
    • A61N1/18—Applying electric currents by contact electrodes
    • A61N1/20—Applying electric currents by contact electrodes continuous direct currents
    • A61N1/30—Apparatus for iontophoresis, i.e. transfer of media in ionic state by an electromotoric force into the body, or cataphoresis

Definitions

  • the present invention relates to an interface for iontophoresis, which allows a drug to electrically penetrate the skin.
  • the present invention relates to a method of effectively absorbing a small amount of a highly active ionotropic bioactive peptide drug to the skin.
  • the present invention relates to an interface for iontophoresis that is suitable for a computer.
  • the present invention also relates to a skin It treatment agent mainly used as a pretreatment at the time of transdermal administration of iontophoresis and a pretreatment method thereof.
  • the present invention relates to an iontophoresis for electrically transmitting a drug to the skin.
  • highly efficient ionic bioactive peptide drugs with trace amounts of high activity, especially bioactive peptides represented by positively charged calcitonin and its analogs, have never been more efficient.
  • the present invention relates to a skin treating agent capable of suppressing adsorption to the skin and effectively absorbing the skin, and a method for treating the same. Background art
  • bioactive peptides are hardly absorbable, hard to absorb an effective amount of drug, and are amphiphilic molecules, so that they are adsorbed to various storage containers when present in an aqueous solution.
  • the recovery from the equipment was poor, and there was a great inconvenience over a small amount of the preparation.
  • containers are conventionally treated with silicone, proteins with relatively low adsorptive activity coexist with these bioactive peptides, and surfactants, carbohydrates, amino acids, etc. are added. By doing so, it has been attempted to prevent adsorption to the storage container (see, for example, JP-A-61-221125 and JP-A-63-57527).
  • Iontophoresis which can control drug permeation, is a percutaneous absorption promotion system that uses electric force.In an electric field created through an anode and a cathode during energization, positively charged molecules move from the anode side to the negative side. This is a therapeutic technique that has been known since the early 1900, in which charged molecules penetrate into the skin layer from the cathode side (J. Controlled Release 1 8. 213-220, 1992) In recent years, the era has come to be re-evaluated as a bioactive peptide administration system. It is known that iontophoresis also improves the transdermal absorption of peptide-based drugs, and much research has been conducted toward its practical use.
  • the interface for iontophoresis as a drug carrier is made of sponge or porous material such as paper, cloth, fibrous synthetic resin continuous foam, or water-absorbent resin.
  • An interface having an aqueous member layer for retaining and holding a chemical solution has been reported, and an interface made of a non-conductive material having a porous body or a porous or capillary structure such as a ceramic has been reported.
  • a bioactive peptide was applied, adhered, coated or impregnated on the interface for iontophoresis, or was placed in a solid or sub-dry state by drying.
  • iontophoresis no drug with sufficient transdermal absorption and satisfactory drug use efficiency has been obtained.
  • the main reason is that these bioactive peptides are not available because they are adsorbed on drug carriers.
  • As a method to solve this problem we have already coated the non-conductive material having a porous or capillary structure with a high molecular protein to prevent the drug from adsorbing to the porous material, Reported a method that can ensure extremely effective transdermal absorption and is also excellent in terms of safety (see Japanese Patent Application Laid-Open No. 6-16353). This method is very effective, but if the coating agent used is an expensive protein, such as BSA (bovine serum albumin), there are stability problems and long-term storage is complicated. Therefore, the development of a more excellent method was required.
  • BSA bovine serum albumin
  • benzalkonium chloride or benzethonium chloride can coexist with a drug-containing solution at a concentration in the range of 0.1-2.0% to prevent adsorption of bioactive peptides to equipment.
  • a drug-containing solution at a concentration in the range of 0.1-2.0% to prevent adsorption of bioactive peptides to equipment.
  • the target drug ions and coexisting ions compete electrically, resulting in a lower translocation rate in drug permeation, resulting in lower utilization efficiency. There is a problem from the purpose of improvement.
  • the amount of these bioactive peptides used in transdermal absorption is so small that the drug is also adsorbed to the skin surface, which is the site of absorption, and it is difficult to accurately control the amount of the bioactive peptide to be injected into the body.
  • bioactive peptide-based drugs have been irreversibly or hardly re-dissolved on the skin / * surface in conventional transdermal drug administration techniques, resulting in inaccurate doses and safety.
  • the present invention provides an inexpensive, stable, and practical interface coating technology for iontophoresis that enhances the reproducibility of the use of bioactive peptide drugs. The purpose is to provide.
  • the present invention also provides an inexpensive and stable practical skin pretreatment technology for iontophoresis by using a cationic surfactant having a disinfecting and disinfecting effect, thereby increasing the drug use efficiency with good reproducibility. Its purpose is to:
  • an interface for iontophoresis comprising a drug holding member and a surface coating layer of an ionizable surfactant formed on the surface of the drug holding member.
  • an iontophoresis transdermal administration skin containing an aqueous solution containing a cationic surfactant or an alcoholic solution for disinfection as a pretreatment agent for the skin of the administration site.
  • a treatment is provided.
  • the skin to be treated is pretreated with an aqueous solution or a disinfecting alcohol solution containing a cationic surfactant having a bactericidal effect.
  • an aqueous solution or a disinfecting alcohol solution containing a cationic surfactant having a bactericidal effect is pretreated with an aqueous solution or a disinfecting alcohol solution containing a cationic surfactant having a bactericidal effect.
  • the drug-adsorbing site on the skin surface is coated, and the drug's membrane permeation efficiency ( A skin pretreatment method that increases the effective utilization rate is provided.
  • FIG. 1 is a plan view of the structure of an applicator device including an interface used in the embodiment.
  • FIG. 2 is a cross-sectional view showing a cross section XX ′ of the structure of FIG. 1, and FIG. 3 is a graph showing test results of Example 1.
  • FIG. 4 is a graph of Example 2 for explaining the present invention, and Group 1 in FIG. 4 shows the time-dependent change in the concentration of calcitonin in the drug solution when the skin was washed only with distilled water. Shows changes over time in the concentration of calcitonin in the drug solution when 9% was washed with a 1% by weight aqueous solution of benzalkonium chloride.
  • FIG. 5 is a graph of Example 3 for explaining the effect of the present invention.
  • Group 3 was treated with calcitonin by iontophoresis after cleaning the skin with 70% by weight ethanol absorbent cotton. Shows the time-dependent change in serum calcium concentration (serum Ca lowering effect) at the time of treatment.
  • Group 4 was treated with 70% by weight ethanol absorbent cotton containing 0.01% by weight benzalkonium chloride, and was washed with ion I tophoresis. The time-dependent change in serum calcium level (calcium lowering effect) when calcitonin was administered is shown.
  • the inventors of the present invention have made intensive efforts to solve the above-described problems, and have prepared a surface of an interface device for iontophoresis having a porous or capillary structure of a non-conductive material, with an ionizing agent for disinfection.
  • an ionizing agent for disinfection for disinfection.
  • the film is coated with a surfactant, the transdermal absorption of the drug is remarkably safe without irritation to skin / sr. And found that the drug use efficiency increased, and as a result of further intensive studies, the present invention was completed.
  • the present invention relates to an interface for iontophoresis in which a coating layer of an ionic surfactant is formed on a drug holding member.
  • the drug holding member is a member that comes into contact with a drug or a drug solution, and has a porous or capillary structure made of a non-conductive material.
  • the above-mentioned ionic surfactant is characterized by being used for preservation and disinfection, and specifically, is a pharmaceutical additive such as benzalkonium chloride, benzethonium chloride, and alkylbenzene sulfonate. It is characterized in that the ionic surfactant is not eluted in the drug solution at the time of use, or even if it is eluted, the concentration is 0.01% by weight or less.
  • the above-mentioned drugs are preferably bioactive peptides which need to increase drug use efficiency.o
  • the drug used in the present invention is not particularly limited as long as it is a pharmaceutically effective bioactive peptide, but the following drugs are exemplified. That is, calcitonin, adrenocorticotropic hormone, parathyroid hormone, inulin, selectin, okintocin, angiotensin, 3—endolphin, glucagon, Vasoprestin, somatosulfin, gastrin, luteinizing hormonal release hormone, enkephalin, neurotensin, atrial sodium diuretic peptide, growth Hormon, Bradykinin, Substance P, Dinolphin, Thyroid-stimulating honolemon, Prolactin, Interferon, Interlokin, G-CSF, Glutathione peroxidase, Superoxide day Smutase, desmopressin, somatomedin, melanophore-stimulated hormone, muramyl dipeptide, bombesin, vasoactive intestine Chi de,
  • the amount of the physiologically active peptides to be added to the liquid composition of the present invention may be an amount sufficient to exhibit the desired medicinal effect, which varies depending on the type of the drug, the weight of the patient, and the symptoms. And may be appropriately selected according to these conditions.
  • the present inventors further cleaned the skin surface to be subjected to iontophoresis transdermal drug administration with an aqueous solution or a disinfecting alcohol solution containing a cationic surfactant having a bactericidal effect in advance. It was found that the coating significantly improved the use efficiency of the drug safely without irritation to the skin, and as a result of further research, the present invention was completed.
  • the surface of the skin is wiped with an aqueous solution containing a cationic surfactant having a disinfecting and disinfecting effect or an alcohol solution for disinfecting, and the drug is used.
  • Efficiency can be improved, and the above cationic surfactant is used as a pharmaceutical additive composed of, for example, benzalkonium chloride, benzene zentium, and the like. If the cationic surfactant is not eluted from the skin or even if it is eluted, the concentration of the treatment solution is 0.01% by weight or less in the drug.If the elution concentration from the skin is high, water is used.
  • a wiping process is performed using the absorbent cotton.
  • a washing treatment method it is possible to enhance the utilization efficiency of a bioactive peptide having a high activity in a small amount, particularly a positively charged peptide (for example, calcitonin).
  • FIGS. 1 and 2 two polyethylene cups (9) and (9 ') are arranged on the upper part of a flexible and rigid support (10). Contains a drug solution (7) composed of distilled water for injection (made by Fuso Pharmaceutical Co., Ltd.) and forms a reservoir (12), and (9) contains, for example, a PVA hydrogel containing NaCl. Built-in conductive gel (3). At the bottom of the support (10)
  • the lower part of (9) is provided with a hole (14) that penetrates the support (10) so that it penetrates the front and back sides when used.
  • the ion exchange membrane (4) for example, AC -220 membrane (made by Asahi Kasei), non-woven fabric (5) (for example, Bemberg (made by Asahi Kasei)), and porous nylon (6) (for example, Bio-Dyne brass (made by Nippon Pall)) It is located in the app
  • the non-woven fabric (5) further extends to the lower part of the support (10) and below the cup (9 '), and the non-woven fabric (5) of the support (10) In the lower part where the non-woven fabric (5) is located, a hole (15) is formed so as to penetrate the front and back sides when used.
  • these drug holding members (the holding in this case includes at least contact with at least May be used as a drug contacting member.) Is treated with a force to uniformly coat or impregnate in a 0.01% benzalkonium chloride aqueous solution, or by immersing them in the same aqueous solution, and drained. This is achieved by drying.
  • the skin of nylon porous material * on the contact surface side, further bioactive peptides Is adhered by means of spray coating, impregnation, etc., and is kept dry.
  • the drug (11) is fixed to the portion of the porous nylon (6) that comes into contact with the living skin (S). Perimeter of nylon porous body (6) An adhesive tape (8) made of, for example, a blender (manufactured by 3M) is arranged below the support (10).
  • the water supply from the reservoir (12) passes through the non-woven fabric (5) having a capillary structure through the opening (15) shown in Fig. 1 and then to the nylon porous body (6). Reach.
  • Energization was performed for 45 minutes at a depolarized constant voltage high frequency pulse of 6 V, 30 kHz, and 30% duty.
  • blood was collected from the jugular vein, centrifuged at 12000 rpm for 5 minutes, and the supernatant was used as a sample serum.
  • Serum calcium was measured by the orthocresol phthalein complexone method (Canoresium C-Test Co., manufactured by Wako Pure Chemical Industries, Ltd.).
  • Example 2 (Test for preventing skin from adsorbing drugs by rat)
  • Hairless razor Male 13-week-old abdominal skin after shaving with a balkan It was rubbed gently with absorbent cotton containing 70% ethanol aqueous solution and disinfected. After exfoliation with scissors, the exfoliated skin was placed on a paper towel soaked with physiological saline so that the epidermis side was facing up. Acryl chamber cups (diameter 18 mm, height 20 mm) were soaked in silicone coating and a 1% aqueous benzalkonium chloride solution for 5 minutes, and then rinsed thoroughly with distilled water. The acrylic chamber cup was adhered to the skin with medical alfalfa and dried. Then, 1% aqueous benzalkonium chloride solution (Group 2) or distilled water (Group 1) was used as a control.
  • the amount of calcitonin in the aqueous solution in a cup of acrylic resin left on the skin after 1 hour was washed with 1% benzalkonium chloride, based on the initially prepared concentration. It was about 60% when treated (Group 2) and about 30% when the skin was washed with distilled water only (Group 1). This is because calcitonin was adsorbed on the rat skin, and the amount of non-adsorbed calcitonin from 2 hours to 6 hours was about 60 to 70% when washed with 1% benzalkonium chloride. Approximately 20-25% of the skin was treated with distilled water alone, and the effect of preventing the adsorption of calcitonin to the skin was observed in the treatment with benzonal conidium chloride.
  • Example 3 Drug transdermal absorption test by rat
  • SD rat male 7 week old abdominal skin was shaved with varican and treated with sliver, and then absorbent cotton containing 70% by weight ethanol aqueous solution (Group 3) or Lightly rub with a cotton wool (Group 4) containing 0.01% benzalkonium chloride in a 70% by weight aqueous ethanol solution and degrease it.
  • Calcitonin synthetic salmon calcitonin, manufactured by SIGMA
  • SIGMA synthetic salmon calcitonin
  • the energization conditions of the iontophoresis were a depolarization type constant voltage high frequency pulse of 6 V, 30 kHz, 30% duty, and energization for 45 minutes. After a predetermined time, blood was collected from the jugular vein, centrifuged at 12000 pm for 5 minutes, and the supernatant was used as a sample serum. The amount of calcium in the blood was measured by the orthocresol phthalein complexone method (calcium C-test Co., Ltd., Wako Pure Chemical Industries, Ltd.).

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Radiology & Medical Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
PCT/JP1995/002000 1994-09-30 1995-09-29 Interface pour administration iontophoretique transcutanee, et agent et methode de traitement de la peau a cette fin WO1996010439A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US08/649,583 US5894021A (en) 1994-09-30 1995-09-29 Iontophoretic transdermal drug-delivery interface and skin treatment agent and treatment method using the same
EP95932949A EP0739644A4 (de) 1994-09-30 1995-09-29 Schnittstelle für eine transdermale iontophoretische vorrichtung und entsprechendes heilmittel

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP6/259677 1994-09-30
JP25967794A JP2818771B2 (ja) 1994-09-30 1994-09-30 イオントフォレーシス用インターフェイス
JP33280694A JP2909483B2 (ja) 1994-12-15 1994-12-15 イオントフォレーシス用皮膚処理剤
JP6/332806 1994-12-15

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WO1996010439A1 true WO1996010439A1 (fr) 1996-04-11

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EP (1) EP0739644A4 (de)
WO (1) WO1996010439A1 (de)

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US5857994A (en) * 1996-10-01 1999-01-12 Becton, Dickinson And Company Awakenable iontophoretic/delivery device for reducing electrical sensation upon application thereof
US6163720A (en) * 1997-12-18 2000-12-19 Alza Corporation Layered rate controlling membranes for use in an electrotransport device
JP4154016B2 (ja) * 1997-12-30 2008-09-24 久光製薬株式会社 イオントフォレーシス装置およびその組み立て方法
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AU2002251541A1 (en) * 2002-04-25 2003-11-10 Centre Pharmapeptides Apparatus and assembly for administering antimicrobial agent
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JP2006116086A (ja) * 2004-10-21 2006-05-11 Tokuyama Corp イオントフォレーシス装置用作用極構造体及びイオントフォレーシス装置
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WO2006055729A1 (en) * 2004-11-16 2006-05-26 Transcutaneous Technologies Inc. Iontophoretic device and method for administering immune response-enhancing agents and compositions
JP4728631B2 (ja) * 2004-11-30 2011-07-20 Ｔｔｉ・エルビュー株式会社 イオントフォレーシス装置
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WO2007026672A1 (ja) * 2005-08-29 2007-03-08 Transcu Ltd. イオントフォレーシス用汎用性電解液組成物
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US20070135754A1 (en) * 2005-09-30 2007-06-14 Hidero Akiyama Electrode assembly for iontophoresis for administering active agent enclosed in nanoparticle and iontophoresis device using the same
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KR20080066712A (ko) * 2005-09-30 2008-07-16 티티아이 엘뷰 가부시키가이샤 관능화된 미세바늘 경피 약물 전달 시스템, 장치 및 방법
WO2007079116A1 (en) * 2005-12-28 2007-07-12 Tti Ellebeau, Inc. Electroosmotic pump apparatus and method to deliver active agents to biological interfaces
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US20080004564A1 (en) * 2006-03-30 2008-01-03 Transcutaneous Technologies Inc. Controlled release membrane and methods of use
US20080058701A1 (en) * 2006-07-05 2008-03-06 Transcutaneous Technologies Inc. Delivery device having self-assembling dendritic polymers and method of use thereof
US20080193514A1 (en) * 2006-11-02 2008-08-14 Transcu Ltd. Compostions and methods for iontophoresis delivery of active ingredients through hair follicles
WO2008087803A1 (ja) * 2007-01-16 2008-07-24 Hokkaido University 抗酸化成分を封入したイオントフォレーシス用リポソーム製剤
MX2009012273A (es) * 2007-05-18 2010-04-09 Tti Ellebeau Inc Dispositivos de suministro transd?rmico que aseguran la liberaci?n mejorada de un principio activo a trav?s de una interfaz biol?gica.
JP2010187707A (ja) * 2007-06-12 2010-09-02 Hokkaido Univ インスリンを封入したイオントフォレーシス用リポソーム製剤
AR073575A1 (es) * 2008-09-10 2010-11-17 Transcu Ltd Aparato y metodo para dispensar basados en hpc liquidos viscosos en sustratos porosos por ejemplo proceso continuo basado en bandas

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Publication number Priority date Publication date Assignee Title
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EP0739644A1 (de) 1996-10-30
US5894021A (en) 1999-04-13

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